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Journal Abstract Search

155 related items for PubMed ID: 9618424

  • 1. Fentanyl and its analogs desensitize the cloned mu opioid receptor.
    Bot G, Blake AD, Li S, Reisine T.
    J Pharmacol Exp Ther; 1998 Jun; 285(3):1207-18. PubMed ID: 9618424
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  • 2. Interaction of p-fluorofentanyl on cloned human opioid receptors and exploration of the role of Trp-318 and His-319 in mu-opioid receptor selectivity.
    Ulens C, Van Boven M, Daenens P, Tytgat J.
    J Pharmacol Exp Ther; 2000 Sep; 294(3):1024-33. PubMed ID: 10945855
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  • 3. Opioid peptide receptor studies. 17. Attenuation of chronic morphine effects after antisense oligodeoxynucleotide knock-down of RGS9 protein in cells expressing the cloned Mu opioid receptor.
    Xu H, Wang X, Wang J, Rothman RB.
    Synapse; 2004 Jun 01; 52(3):209-17. PubMed ID: 15065220
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  • 5. Endogenous regulator of g protein signaling proteins reduce {mu}-opioid receptor desensitization and down-regulation and adenylyl cyclase tolerance in C6 cells.
    Clark MJ, Traynor JR.
    J Pharmacol Exp Ther; 2005 Feb 01; 312(2):809-15. PubMed ID: 15383633
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  • 9. Synthesis and pharmacological studies of new hybrid derivatives of fentanyl active at the mu-opioid receptor and I2-imidazoline binding sites.
    Dardonville C, Fernandez-Fernandez C, Gibbons SL, Ryan GJ, Jagerovic N, Gabilondo AM, Meana JJ, Callado LF.
    Bioorg Med Chem; 2006 Oct 01; 14(19):6570-80. PubMed ID: 16797997
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  • 10. Differences in tolerance to anti-hyperalgesic effects between chronic treatment with morphine and fentanyl under a state of pain.
    Imai S, Narita M, Hashimoto S, Nakamura A, Miyoshi K, Nozaki H, Hareyama N, Takagi T, Suzuki M, Narita M, Suzuki T.
    Nihon Shinkei Seishin Yakurigaku Zasshi; 2006 Nov 01; 26(5-6):183-92. PubMed ID: 17240843
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  • 12. Role of cAMP-dependent protein kinase (PKA) in opioid agonist-induced mu-opioid receptor downregulation and tolerance in mice.
    Shen J, Benedict Gomes A, Gallagher A, Stafford K, Yoburn BC.
    Synapse; 2000 Dec 01; 38(3):322-7. PubMed ID: 11020235
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  • 15. delta-Opioid receptors are more efficiently coupled to adenylyl cyclase than to L-type Ca(2+) channels in transfected rat pituitary cells.
    Prather PL, Song L, Piros ET, Law PY, Hales TG.
    J Pharmacol Exp Ther; 2000 Nov 01; 295(2):552-62. PubMed ID: 11046088
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  • 16. Ultra-low-dose naloxone suppresses opioid tolerance, dependence and associated changes in mu opioid receptor-G protein coupling and Gbetagamma signaling.
    Wang HY, Friedman E, Olmstead MC, Burns LH.
    Neuroscience; 2005 Nov 01; 135(1):247-61. PubMed ID: 16084657
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  • 17. Human mu-opioid receptor overexpressed in baculovirus system and its pharmacological characterizations.
    Wei Q, Zhou DH, Shen QX, Wang CH, Chen J, Li CL, Pei G, Chi ZQ.
    Zhongguo Yao Li Xue Bao; 1998 May 01; 19(3):218-22. PubMed ID: 10375729
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